A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362236



Internal ID21019789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155582019..155582276hg38UCSC Ensembl
chr3:155299808..155300065hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38258
hg19258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096434
Samples
Known GenesPLCH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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